Singapore | Posted: Jun 10, 2025

Plan and prioritize the Pre-Production aspects of the packaging of clinical trial supplies, including:
Creation of accurate Pack Designs that reflect the needs of the client and meet GMP requirements.
Ensure appropriate QIF’s are raised in the event that final Pack Designs differ from the original contract.
Procurement with Approved vendors to purchase required packaging components, label stock and equipment in a timely manner to hit Production timelines
Working closely with the Project Management team to ensure good understanding of the projects and that all client required documentation is received and approved in a timely manner e.g. Label Approvals
Working with the Centre of Excellence for Label Printing (SCH) to organize the set-up of new labels within the Clinicopia label printing system and to set-up local label printing jobs
Set-up of packaging configurations and packaging jobs within the Global Scan Assembly system
Creation of accurate packaging and labeling documentation to meet the needs of both the client and regulatory GMP requirements including Label Print Forms (LPF’s) and Batch Records (automated via SupplyFlex and manual)
Creation of example packs and blinding samples in line with SOP’s
Identify and implement cost, quality, service and safety improvements within the Pre-Production areas
Identify continuous improvement opportunities & delivery of improvement actions to continually enhance the performance of the team
Review/approve documentation prepared by other staff
Ensure that all work is carried out in compliance with current Good Manufacturing Practice and Health and Safety requirements
Any other duties which may properly be assigned to this post.
Requirement : 
Min N/O Level 
Some 1-3 years logistics experiences